Gene · 55636
Papers2,784
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1 to 20 of 2,784
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Epigenetic role of miR-574 in sperm chromatin remodeling and developmental gene networks in male infertility. | Reprod Fertil Dev | 2026 | 42816179 | PubTator, text mining | PubMed |
| Chromodomain helicase DNA-binding proteins and orofacial cleft. | J Res Med Sci | 2026 | 42808081 | PubTator, text mining | PubMed |
| The Runx1-Gata2 axis: epigenetic architecture of lineage fate. | Mol Biol Rep | 2026 | 42801378 | PubTator, text mining | PubMed |
| A CHD7 intronic variant induces aberrant splicing and structural alterations in the CHD7 DNA-binding domain to cause CHARGE syndrome. | Am J Transl Res | 2026 | 42769338 | PubTator, text mining | PubMed |
| Genetic Heterogeneity of Inborn Errors of Immunity Revealed by Whole-Genome Sequencing: Insights from a Russian Patient Cohort. | Int J Mol Sci | 2026 | 42737820 | PubTator, text mining | PubMed |
| Comprehensive Analysis of Cuproptosis-Related Genes According to Cancer Stage and Their Prognostic Value in Cervical Cancer. | Int J Mol Sci | 2026 | 42737631 | PubTator, text mining | PubMed |
| Case Report: Differential outcomes associated with the same pathogenic variant: long-term follow-up of a CHARGE syndrome case with a nonsense mutation c.6292C>T in the CHD gene. | Front Genet | 2026 | 42733771 | PubTator, text mining | PubMed |
| Dual Aberrant Splicing Caused by an Apparently Missense CHD7 Variant, c.5273A>G (p.Asp1758Gly), in CHARGE Syndrome. | Am J Med Genet A | 2026 | 42733123 | PubTator, text mining | PubMed |
| ATRX Condensates as Candidate Organizers of Enhancer-Centered Nuclear Microenvironments in Neural Progenitors: A Hypothesis for Enhancer-Associated ATRX Function in Neural Progenitors. | Bioessays | 2026 | 42725378 | PubTator, text mining | PubMed |
| Metabolomic analysis of children with congenital heart disease complicated by neurological developmental abnormalities and CHD7 mutations. | Front Genet | 2026 | 42725350 | PubTator, text mining | PubMed |
| Developmental senescence misregulation in congenital disorders: CHARGE syndrome as a candidate model. | Aging (Albany NY) | 2026 | 42715611 | PubTator, text mining | PubMed |
| Immunological characteristics of calmodulin-related genes in hepatocellular carcinoma and their potential for prognostic prediction and diagnostic applications. | J Gastrointest Oncol | 2026 | 42703336 | PubTator, text mining | PubMed |
| Spinal Involvement in Charge Syndrome: Implications for Management. | Am J Med Genet A | 2026 | 42675809 | PubTator, text mining | PubMed |
| [Clinical phenotype and genetic analysis of 7 neonates with CHARGE syndrome caused by CHD7 gene variants]. | Zhongguo Dang Dai Er Ke Za Zhi | 2026 | 42608301 | PubTator, text mining | PubMed |
| Genotypic and Phenotypic Profile of 50 Cases With Chromatin Remodeling Complexes-Related Neurological Disorders. | CNS Neurosci Ther | 2026 | 42528014 | PubTator, text mining | PubMed |
| Centrosome-related gene SPHK1 drives bladder cancer progression and therapeutic vulnerability. | Transl Oncol | 2026 | 42485786 | PubTator, text mining | PubMed |
| The Spectrum of Congenital Hypogonadotropic Hypogonadism: A 30-Year Experience at a Tertiary Paediatric Centre. | Clin Endocrinol (Oxf) | 2026 | 42485653 | PubTator, text mining | PubMed |
| Dental Management of CHARGE Syndrome Under General Anaesthesia: A Case Report. | Spec Care Dentist | 2026 | 42478163 | PubTator, text mining | PubMed |
| Novel CHD7 Variants Associated with an Expanded Orofacial and Dental Phenotype. | Eur J Dent | 2026 | 42457132 | PubTator, text mining | PubMed |
| Evaluating the prognostic value of cuproptosis-related genes and characterizing PDE3B's role in gastric cancer: integrative bioinformatics analysis and experimental validation. | J Gastrointest Oncol | 2026 | 42434223 | PubTator, text mining | PubMed |
gene-search-2026-11-11-0.2.0
Sources 12
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
- GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
- HGNCCC0
- NCBI GenePublic domain (US government)
- NIH's project files and grant-paper linksPublic domain
- Open TargetsCC0 1.0
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
- GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
- HGNCCC0: https://www.genenames.org/about/license/
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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